Clinical Trials Jobs in Oxfordshire
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Production Development Engineer
- Salary:
- £40-50K
- Location:
- Oxfordshire
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 11:32Add to My Shortlist
We have an exciting opportunity to work for a medical device company with cutting edge technology that specialises in monitoring systems. The organisation is looking for a Production Development Engineer with knowledge of continuous improvement techniques and a chemical background. You will need process engineering knowledge of medical devices or pharmaceutical process development within a variety of applications. The individual... validation of process and equipment *Writing and updating work instructions *Maintaining records *Acceptance and rejection of raw materials and control changes to production process *Carry out risk assessment for production equipment and tooling The ideal candidate will be tasked to take manufacturing systems which is used in first Human Use Clinical trials to Gen 2 Device manufacturing system. He or she will be responsible for jigs and automate where possible in addition to scale up old processes in the company's new premises. You must be a "hands on" person that can strip down and rebuild equipment. In addition my client is offering...
Clinical Research Physician - Oncology, UK
- Salary:
- Excellent + Benefits
- Location:
- Berkshire, Buckinghamshire, Oxfordshire, Hampshire, London, Surrey, Uk
- Job Type:
- Any
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
Clinical Research Physician - Oncology My client, a leading pharmaceutical organisation with an international presence are looking to recruit a pharmaceutical physician with a background in Oncology at either Associate Director or Director level. Role Detail: Working in a Uk-based role, but as part of a global team, you will be responsible for the management and development of PI -... This is a permanent, office-based role with some international travel when required. To Apply: Please call Toby Ferguson at Only Medics on +44 (0) 1189 522799 or e-mail your CV to toby@onlymedics.com. All applications will be held in absolute confidence. Keywords: medic physician doctor research physician medical affairs clinical development clinical trials pharmacovigilance drug safety GMC Phase I Phase II Phase III Oncology Haematology Hematology Onco-Haematology Haemato-Oncology Cancer Berkshire Buckinghamshire Bedfordshire Hampshire Hertfordshire Middlesex London Surrey UK anywhere re-locate
Biometrics Team Leader
- Salary:
- On application
- Location:
- London, Buckinghamshire, Oxfordshire, Hampshire, Berkshire, Surrey, Middlesex
- Job Type:
- Contract/Interim
- Date Posted:
- 30-May-2012 00:00Add to My Shortlist
BIOMETRICS TEAM LEADER (BASED IN: LONDON) (SALARY: ON APPLICATION) The is a new and exciting opportunity for a Biometrics Team Leader (Data Manager), to join an expanding company involved in Phases I-IV trials including Pharmacokinetic studies in patients and healthy volunteer studies. Initially a 6 Month Contract, working 3 days per week, based in the London area. As Biometrics Team Leader, you will be responsible for ensuring that all data management and statistical activities are conducted in accordance with the clinical trials legislation and guidelines. You will manage, co-ordinate, oversee and deliver all data management and statistical activities and provide leadership and management of personnel associated with these activities. MAJOR RESPONSIBILITIES *To act as the primary contact for data management, statistics, monitoring and regulatory personnel (the Team) in terms of Biometrics *To...
Pharmacovigilance Lead - UK
- Salary:
- £Excellent + Benefits
- Location:
- South England, South East England, Surrey, Berkshire, Oxfordshire, Middlesex, London, Kent, Buckinghamshire
- Job Type:
- Any
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
Pharmacovigilance Lead - UK Client: One of the worlds leading Pharmaceutical Companies based near the M4 corridor are recruiting for a Global Pharmacovigilance Lead. This is a great opportunity to join a rapidly growing department and offer first rate career progression for a high calibre candidate. Description: The Global Pharmacovigilance Lead will report to and assist the Therapeutic Area Director... drugs that are marketed and/or in clinical development. The successful candidate will help ensure proactive and timely assessments of safety data to characterize the emerging and known safety profiles of the products within the Therapy Area. Required technical knowledge and skills *Ability to critically evaluate safety data from multiple sources (clinical trials, environment, literature, etc), assess clinical importance and potential strategic impact of the data and present the findings clearly in both written and oral communications. *Experience and knowledge of Good Clinical Practices and Pharmacovigilance regulatory requirements in US, the EU and globally, the conduct of clinical trials and for the appropriate contributions...
Medical Information Specialist
- Salary:
- £Negotiable + Benefits
- Location:
- Berkshire, Hampshire, Middlesex, Hertfordshire, Surrey, London, Oxfordshire, Buckinghamshire, South England, South East England
- Job Type:
- Any
- Date Posted:
- 25-May-2012 10:25Add to My Shortlist
Medical Information Specialist Berkshire Excellent salary and benefits Leading pharmaceutical company is looking for a Medical Information Specialist. A key component of this role is handling enquiries from external customers. As such a Medical Information Specialist will have telephone contact with external customers including Healthcare Professionals, patients, carers and competitor companies, as required. KEY ACTIVITIES *Answer telephone, web-based and written enquiries from health care professionals, members of the public and internal customers concerning the safe and effective use of all products marketed by the company in a timely manner *Record all external customer contacts in the database *Search relevant data sources, both internal and external, to identify and retrieve relevant data and information...
CRA Line Manager
- Salary:
- £Negotiable + Benefits
- Location:
- Berkshire, Buckinghamshire, Oxfordshire, Middlesex, London, Hertfordshire, Hampshire, Surrey, Bedfordshire, South East England
- Job Type:
- Any
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
CRA Line Manager Office based in Buckinghamshire Industry leading salary plus excellent benefits package A fantastic senior position has arisen for an ambitious, articulate and highly driven CRA Manager to be office based in Buckinghamshire. You will be joining a prestigious pharmaceutical company that has forged a solid reputation for developing innovative products across a number of speciality markets. This position will require the candidate to lead, manage, develop and motivate Clinical Research Associates across Europe to deliver on all clinical trial commitments in a specific geographical area. You will report directly to the Director of Global Development Operations and will provide a single point of contact for the TA teams and other stakeholders for the region. The candidate will be responsible for a number of deliverables including: *Resourcing plan *Budget proposal...
Regulatory Affairs Officer
- Salary:
- £Negotiable + Benefits
- Location:
- Berkshire, Hampshire, Middlesex, Surrey, London, Hertfordshire, Buckinghamshire, Oxfordshire, South East England
- Job Type:
- Any
- Date Posted:
- 23-May-2012 14:04Add to My Shortlist
Regulatory Affairs Officer Location: Berkshire Employment term: Permanent Salary: Competitive A fantastic opportunity has arisen for a Regulatory Affairs Officer to join a global pharmaceutical company based in Berkshire. The Regulatory Affairs Officer will provide advice and support to the UK, Ireland and Malta affiliate. As Regulatory Affairs Officer you will focus on post approval work and labelling activities, as well as regularly deal with the MHRA. Responsibilities include; *Gaining regulatory authority approval for new clinical trials and amendments to such trials undertaken in the UK. *Gaining Marketing Authorisation Applications for new pharmaceutical products in the UK, Ireland and Malta where applicable. *Compiling variations and renewals for current Marketing Authorisation Applications. *Liaise with European Regulatory Affairs and Corporate groups on regulatory issues. *Draft of packaging texts, SmPC's, ...
Senior Medical Advisor - CNS - Movement Disorders
- Salary:
- On Application
- Location:
- Bedfordshire, Berkshire, Buckinghamshire, Essex, Hertfordshire, Oxfordshire, Surrey, London, Hampshire, Kent, Middlesex, West Sussex
- Job Type:
- Permanent
- Date Posted:
- 23-May-2012 09:05Add to My Shortlist
JOB SUMMARY Leading Global Biopharma. We are looking for a Senior Medical Advisor to support their products in the Movement Disorder CNS area. Based in Berkshire - full time role. BACKGROUND Our client is a biopharma leader dedicated to the research, development and commercialisation of medicines to treat patients suffering from severe diseases. With a unique combination of expertise in... product as an integral member of the UK brand team and will work closely with the global medical and commercial teams. The role will involve the development of strong relationships with top opinion leaders in the field, the development of Phase IV trials and support for locally and globally coordinated clinical trials in the UK. The company can provide extensive opportunities for career development. As a mid-sized company, with global resources, they're small enough for each member of the team to feel that their contribution counts and large enough to ensure that their combined efforts have an impact where it really matters....
EU Associate Director Medical Affairs Transplantation
- Salary:
- On Application
- Location:
- Cambridgeshire, Bedfordshire, Berkshire, Essex, Hertfordshire, Oxfordshire, Surrey, London, East Sussex, Hampshire, Kent, Middlesex, West Sussex
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:10Add to My Shortlist
Benefits: Competitive salary and bonus scheme, car, health, life cover, pension JOB SUMMARY Excellent opportunity for a GMC registered medic with speciality training in clinical transplantation, nephrology or hepatology to step up to a European role to support products in the Transplantation area. BACKGROUND One of the world's top 20 pharmaceutical companies, our client is a growing, forward-thinking organisation, rich...
Line Manager, Clinical Operations
- Salary:
- £excellent
- Location:
- Field Based, Uk, Berkshire, Oxfordshire, Buckinghamshire, Hampshire, Hertfordshire, London, Surrey, Wiltshire
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
Line Manager, Clinical Operations Field Based UK £excellent salary + full benefits My client is a market leading pharmaceutical services organisation with a superb track record of delivering a large number of blockbuster medicines. With a number of recent business wins and experiencing unparalleled growth in the UK they are looking to recruit an experienced line manager to join their... successful candidate will be an experienced and highly motivated Clinical Research professional with a proven track record in people management. They will be accountable for ensuring delivery of key projects to time, quality and budget through the successful management of a team comprising; clinical study managers; clinical research associates and clinical trial assistants. The Clinical Operations Manager will be responsible for recruiting, developing and maintaining the professional standard, quality and consistency of their team. To be considered for this position it is important that you have a bachelor's degree in a health care or other scientific discipline complimented by previous of experience...
Regulatory Affairs Executive/ Senior Regulatory Affairs Executive
- Salary:
- On Application
- Location:
- Berkshire, Oxfordshire, Surrey, London
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:06Add to My Shortlist
JOB SUMMARY A fantastic opportunity for a Regulatory Executive looking to work within a global pharmaceutical company. You will operate with some supervision (depending on experience) providing regulatory support to the UK and Ireland portfolio. Experience with post marketed products is essential. BACKGROUND Global ethical Pharmaceutical company PRIMARY DUTIES * Ensure all Marketing Authorizations they are responsible for are kept... (Medical Information, Pharmacovigilance, Commercial etc). * Provide support to improve and document Regulatory Department processes and other special projects as required. * Proactively build relationships externally (MHRA/IMB) and internally, so that business needs are met. * Support the Global regulatory group in the preparation and submission of licence applications and clinical trial applications within agreed timelines. * Manage relationship with external 3rd parties (e.g. contract manufacturers). * Ensure license changes are communicated in a timely manner with Quality Assurance. QUALIFICATIONS / EXPERIENCE REQUIRED: * Experience in regulatory affairs, preferably including experience in some of the following: Marketing Authorisation Applications, marketed products, variations, ...
Senior Clinical Data Manager
- Salary:
- £40, 000
- Location:
- South East, Brighton, Canterbury, Chichester, Dover, Hastings, Oxford, Portsmouth, Southampton, Maidstone, Reading,
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 12:20Add to My Shortlist
CK Clinical are currently recruiting for a Senior Clinical Data Manager to work for a leading Pharmaceutical company in the South-East, whereby you will be responsible for all Data Management activities, including data quality and the timely delivery of database locks for projects, particularly within the Oncology therapy area. You will perform all DM activities (including set-up, managing the Data... in providing Data Management support for Oncology studies, setting up and management of EDC studies using either Inform or Clintrial and proven experience in handling local laboratory data. You will have thorough knowledge and understanding of GCP, the clinical research drug development process and the role of Data Management in clinical trials and proven experience in managing CROs, internal project teams and external vendors. CK Clinical is an Equal Opportunities employer and welcomes applications from al who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that...
Senior Manager Regulatory Affairs
- Salary:
- On Application
- Location:
- Berkshire, Oxfordshire, London, Surrey, Wiltshire, Hampshire, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: Fantastic opportunity for an experienced Regulatory Affairs specialist to take responsibility for management of Regulatory Affairs activities relating to one or more products. You will also be responsible for obtaining and maintaining the required regulatory approvals for those products, including clinical trial approvals and provide strategic regulatory advice to project teams in relation to product development (manufacturing, safety, non-clinical) and clinical development, Phase I through to licensure. BACKGROUND: As a global biopharmaceutical company, our client pursues the development, manufacture and commercialization of vaccines and therapeutics that target infectious diseases, oncology and autoimmune...
Medical Affairs - Clinical Research Nurse Jobs in Reading
- Salary:
- £25,000 pa
- Location:
- Berkshire, Reading, Bracknell, Maidenhead, Newbury, Windsor, Wokingham, Abingdon
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 11:58Add to My Shortlist
Medical Affairs - Clinical Research Nurse Job in Reading Competitive Salary - Full Time - Maternity Cover Is it time for a change from NHS nursing? Do you wish to broaden your experience and develop your career with one of the worlds leading organisations in the field of Clinical Research? Do you want to be involved in groundbreaking research and... for Clinical Research Nurses to become an integral part of their ever evolving and varied research programs. Job Title Clinical Research Nurse Background As a vital part of the study team, Clinical Research Nurses are responsible for planning and implementing the practical aspects of a clinical study, and ensuring the health and safety of human volunteers. Key Responsibilities - Volunteer supervision. - Volunteer recruitment and screening. - Performing clinical procedures (recording vital signs, recording vital signs, collecting and processing blood samples, collecting biological samples). - Data collection and recording. - Compiling study related guidelines. - Ordering study supplies. Qualifications and Experience...
Regulatory Affairs Specialist
- Salary:
- £30,000 - £35,000pa
- Location:
- South West England, Berkshire, Oxfordshire, London, Surrey, Wiltshire, Hampshire
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 00:00Add to My Shortlist
Job Summary: Regulatory Affairs Specialist Excellent opportunity for an experienced Regulatory Affairs Specialist to join the Regulatory Affairs team of a successful UK Biopharmaceutical company. This is a contract role to cover maternity leave for up to a year. Main Duties: Our client, a Biopharmaceutical company who specialise in the development and manufacture of therapeutics that target the treatment of CNS disorders and Oncology, are seeking a Regulatory Affairs Specialist to join their team. Preparation of clinical trial documents for submission to regulatory authorities in countries worldwide. Preparation of marketing authorisation applications Maintenance activities. Provide regulatory support to the team. Qualifications / Experience Required: Life-science degree Experience within a regulatory environment Excellent communication skills, both written and verbal. Able to manage own workload Well-organised with an excellent attention...